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Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis

Complex regulatory programs control cell adaptation to environmental changes by setting condition‐specific proteomes. In balanced growth, bacterial protein abundances depend on the dilution rate, transcript abundances and transcript‐specific translation efficiencies. We revisited the current theory...

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Autores principales: Borkowski, Olivier, Goelzer, Anne, Schaffer, Marc, Calabre, Magali, Mäder, Ulrike, Aymerich, Stéphane, Jules, Matthieu, Fromion, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683663/
https://www.ncbi.nlm.nih.gov/pubmed/27193784
http://dx.doi.org/10.15252/msb.20156608
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author Borkowski, Olivier
Goelzer, Anne
Schaffer, Marc
Calabre, Magali
Mäder, Ulrike
Aymerich, Stéphane
Jules, Matthieu
Fromion, Vincent
author_facet Borkowski, Olivier
Goelzer, Anne
Schaffer, Marc
Calabre, Magali
Mäder, Ulrike
Aymerich, Stéphane
Jules, Matthieu
Fromion, Vincent
author_sort Borkowski, Olivier
collection PubMed
description Complex regulatory programs control cell adaptation to environmental changes by setting condition‐specific proteomes. In balanced growth, bacterial protein abundances depend on the dilution rate, transcript abundances and transcript‐specific translation efficiencies. We revisited the current theory claiming the invariance of bacterial translation efficiency. By integrating genome‐wide transcriptome datasets and datasets from a library of synthetic gfp‐reporter fusions, we demonstrated that translation efficiencies in Bacillus subtilis decreased up to fourfold from slow to fast growth. The translation initiation regions elicited a growth rate‐dependent, differential production of proteins without regulators, hence revealing a unique, hard‐coded, growth rate‐dependent mode of regulation. We combined model‐based data analyses of transcript and protein abundances genome‐wide and revealed that this global regulation is extensively used in B. subtilis. We eventually developed a knowledge‐based, three‐step translation initiation model, experimentally challenged the model predictions and proposed that a growth rate‐dependent drop in free ribosome abundance accounted for the differential protein production.
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spelling pubmed-56836632017-11-20 Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis Borkowski, Olivier Goelzer, Anne Schaffer, Marc Calabre, Magali Mäder, Ulrike Aymerich, Stéphane Jules, Matthieu Fromion, Vincent Mol Syst Biol Articles Complex regulatory programs control cell adaptation to environmental changes by setting condition‐specific proteomes. In balanced growth, bacterial protein abundances depend on the dilution rate, transcript abundances and transcript‐specific translation efficiencies. We revisited the current theory claiming the invariance of bacterial translation efficiency. By integrating genome‐wide transcriptome datasets and datasets from a library of synthetic gfp‐reporter fusions, we demonstrated that translation efficiencies in Bacillus subtilis decreased up to fourfold from slow to fast growth. The translation initiation regions elicited a growth rate‐dependent, differential production of proteins without regulators, hence revealing a unique, hard‐coded, growth rate‐dependent mode of regulation. We combined model‐based data analyses of transcript and protein abundances genome‐wide and revealed that this global regulation is extensively used in B. subtilis. We eventually developed a knowledge‐based, three‐step translation initiation model, experimentally challenged the model predictions and proposed that a growth rate‐dependent drop in free ribosome abundance accounted for the differential protein production. John Wiley and Sons Inc. 2016-05-18 /pmc/articles/PMC5683663/ /pubmed/27193784 http://dx.doi.org/10.15252/msb.20156608 Text en © 2016 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Borkowski, Olivier
Goelzer, Anne
Schaffer, Marc
Calabre, Magali
Mäder, Ulrike
Aymerich, Stéphane
Jules, Matthieu
Fromion, Vincent
Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
title Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
title_full Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
title_fullStr Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
title_full_unstemmed Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
title_short Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
title_sort translation elicits a growth rate‐dependent, genome‐wide, differential protein production in bacillus subtilis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683663/
https://www.ncbi.nlm.nih.gov/pubmed/27193784
http://dx.doi.org/10.15252/msb.20156608
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